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. 2020 Oct 22;10:532292. doi: 10.3389/fonc.2020.532292

Table 1.

Table summarizing the H1299 and H1299-LKB1 KO 1 clone (here reported as LKB1 KO 1) IC50 of the eleven hit compounds from the drug library screening.

DRUG CLASS H1299 IC50 (μM) LKB1 KO 1 IC50 (μM) IC50 H1299 / IC50 LKB1 KO 1
Birinapant IAP inhibitor >5 0.527
(0.466–0.596)
≥9.48
6-Mercaptopurine Antimetabolite >5 0.212
(0.184–0.244)
≥2.36
Clofarabine Antimetabolite 0.717
(0.559–0.954)
0.332
(0.289–0.385)
2.16
Floxuridine Antimetabolite 0.106
(0.065–0.178)
0.054
(0.038–0.789)
1.95
Pitavastatin Calcium HMG-CoA reductase inhibitor 3.114
(1.681–13.159)
1.687
(1.028–3.877)
1.84
Fostamatinib SYK inhibitor 4.380
(3.904–5.156)
2.660
(2.506–2.819)
1.65
Chloroxine Antibacterial 3.399
(3.138–3.682)
3.100
(2.878–3.326)
1.10
Disulfiram ADLH-inhibitor 0.241
(0.136–0.412)
0.289
(0.159–0.514)
0.83
Chlorhexidine HCl Antiseptic 0.747
(0.626–0.876)
1.942
(1.792–2.101)
0.39
Cobimetinib MEK inhibitor >4 >4
Pimasertib MEK inhibitor >4 >4

For each compound the drug class, the IC50 in the two cell lines and the ratio between the IC50 in the H1299 and H1299-LKB1 KO 1 clone are indicated.